EP0261885A1 - Glaszusammensetzungen - Google Patents
Glaszusammensetzungen Download PDFInfo
- Publication number
- EP0261885A1 EP0261885A1 EP87308279A EP87308279A EP0261885A1 EP 0261885 A1 EP0261885 A1 EP 0261885A1 EP 87308279 A EP87308279 A EP 87308279A EP 87308279 A EP87308279 A EP 87308279A EP 0261885 A1 EP0261885 A1 EP 0261885A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- glass composition
- borosilicate glass
- amount
- composition according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 61
- 239000011521 glass Substances 0.000 title claims abstract description 44
- 239000005388 borosilicate glass Substances 0.000 claims abstract description 36
- GOLCXWYRSKYTSP-UHFFFAOYSA-N Arsenious Acid Chemical compound O1[As]2O[As]1O2 GOLCXWYRSKYTSP-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims abstract description 14
- CETPSERCERDGAM-UHFFFAOYSA-N ceric oxide Chemical compound O=[Ce]=O CETPSERCERDGAM-UHFFFAOYSA-N 0.000 claims abstract description 14
- 229910000422 cerium(IV) oxide Inorganic materials 0.000 claims abstract description 14
- 229910011255 B2O3 Inorganic materials 0.000 claims abstract description 8
- FUJCRWPEOMXPAD-UHFFFAOYSA-N Li2O Inorganic materials [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 claims abstract description 8
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims abstract description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims abstract description 8
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000003513 alkali Substances 0.000 claims abstract description 7
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Inorganic materials O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 claims abstract description 7
- 230000001681 protective effect Effects 0.000 claims abstract description 7
- YEAUATLBSVJFOY-UHFFFAOYSA-N tetraantimony hexaoxide Chemical compound O1[Sb](O2)O[Sb]3O[Sb]1O[Sb]2O3 YEAUATLBSVJFOY-UHFFFAOYSA-N 0.000 claims abstract description 7
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 claims abstract description 5
- 229910052681 coesite Inorganic materials 0.000 claims abstract description 4
- 229910052906 cristobalite Inorganic materials 0.000 claims abstract description 4
- 239000000377 silicon dioxide Substances 0.000 claims abstract description 4
- 235000012239 silicon dioxide Nutrition 0.000 claims abstract description 4
- 229910052682 stishovite Inorganic materials 0.000 claims abstract description 4
- 229910052905 tridymite Inorganic materials 0.000 claims abstract description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 30
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 12
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 8
- 229910052593 corundum Inorganic materials 0.000 claims description 5
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 5
- 230000005540 biological transmission Effects 0.000 description 12
- 229910000420 cerium oxide Inorganic materials 0.000 description 12
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 10
- 230000005855 radiation Effects 0.000 description 10
- 229910052684 Cerium Inorganic materials 0.000 description 8
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 8
- 238000005191 phase separation Methods 0.000 description 7
- 238000010521 absorption reaction Methods 0.000 description 6
- 238000002844 melting Methods 0.000 description 6
- 230000008018 melting Effects 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 238000007670 refining Methods 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- 239000010703 silicon Substances 0.000 description 5
- 239000004408 titanium dioxide Substances 0.000 description 5
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 3
- 229910000410 antimony oxide Inorganic materials 0.000 description 3
- 229910000413 arsenic oxide Inorganic materials 0.000 description 3
- 229910001947 lithium oxide Inorganic materials 0.000 description 3
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 description 3
- 238000002203 pretreatment Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910000287 alkaline earth metal oxide Inorganic materials 0.000 description 2
- DRVWBEJJZZTIGJ-UHFFFAOYSA-N cerium(3+);oxygen(2-) Chemical class [O-2].[O-2].[O-2].[Ce+3].[Ce+3] DRVWBEJJZZTIGJ-UHFFFAOYSA-N 0.000 description 2
- 238000012505 colouration Methods 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 229910001948 sodium oxide Inorganic materials 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- -1 MgO Chemical compound 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 229960002594 arsenic trioxide Drugs 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229940044927 ceric oxide Drugs 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- KTTMEOWBIWLMSE-UHFFFAOYSA-N diarsenic trioxide Chemical compound O1[As](O2)O[As]3O[As]1O[As]2O3 KTTMEOWBIWLMSE-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000007496 glass forming Methods 0.000 description 1
- 239000000156 glass melt Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910001950 potassium oxide Inorganic materials 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/11—Glass compositions containing silica with 40% to 90% silica, by weight containing halogen or nitrogen
- C03C3/112—Glass compositions containing silica with 40% to 90% silica, by weight containing halogen or nitrogen containing fluorine
- C03C3/115—Glass compositions containing silica with 40% to 90% silica, by weight containing halogen or nitrogen containing fluorine containing boron
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C4/00—Compositions for glass with special properties
- C03C4/08—Compositions for glass with special properties for glass selectively absorbing radiation of specified wave lengths
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/089—Glass compositions containing silica with 40% to 90% silica, by weight containing boron
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C3/00—Glass compositions
- C03C3/04—Glass compositions containing silica
- C03C3/076—Glass compositions containing silica with 40% to 90% silica, by weight
- C03C3/095—Glass compositions containing silica with 40% to 90% silica, by weight containing rare earths
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/04—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof adapted as photovoltaic [PV] conversion devices
- H01L31/042—PV modules or arrays of single PV cells
- H01L31/048—Encapsulation of modules
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S501/00—Compositions: ceramic
- Y10S501/90—Optical glass, e.g. silent on refractive index and/or ABBE number
- Y10S501/905—Ultraviolet transmitting or absorbing
Definitions
- the present invention relates to borosilicate glass compositions. More particularly, the invention relates to borosilicate glass compositions which incorporate cerium oxide and which are suitable for use as protective covers for solar cells, especially solar cells used in satellites.
- Glass compositions which are intended for use as protective covers for solar cells must have a number of optical characteristics. Such glass compositions must, inter alia, exhibit the following properties:
- Borosilicate glasses are found to have coefficients of linear expansion which are of the desired value.
- cerium oxide tends to induce phase separation in the glass and also tends to impart a yellow to brown colouration in the glass thereby impairing the high white light transmission of the glass.
- the present invention aims to overcome these drawbacks by providing a class of borosilicate glass compositions which contain 2.0% by weight or more of CeO2, in the presence of antimony oxide and/or arsenic oxide.
- the present invention provides a low alkali borosilicate glass composition
- a low alkali borosilicate glass composition comprising 60 to 78% by weight of SiO2 10 to 25% by weight of B2O3 3.5 to 6.0% by weight of R2O, wherein R2O represents Na2O, K2O and/or Li2O, 2.0 to 6.5% by weight of CeO2, and 0.25 to 8.0% by weight of Sb2O3 and/or As2O3, the percentages being based on the total weight of the glass composition.
- Cerium oxide (ceria) is necessary to impart the required UV absorption and radiation stability to the borosilicate glass compositions. Ceria is always expressed as ceric or cerium 4 oxide, even though it is generally present in the glass as a mixture of ceric and cerous (cerium 3) oxides, and may even be present wholly as cerium 3 oxide.
- cerium oxides It is difficult to incorporate large quantities of cerium oxides into low-alkali borosilicate glass compositions owing to the tendency of cerium to promote phase separation, and the maximum cerium levels can only be used with boric oxide levels below about fifteen percent. Cerium oxides also tend to impart a yellow to brown colouration to known borosilicate glass compositions, and it is difficult to combine the maximum UV absorption with good white light transmission. For example, if ceric oxide is added to a typical commercial low-expansion borosilicate glass of the type known as Pyrex, then the glass becomes darkly coloured with cerium oxide contents exceeding about two percent and the glasses will be unsuitable for use as solar cell covers.
- the quantity of cerium oxide can be increased above 2% by weight if the glass composition incorporates Sb2O3 and/or As2O3 in a total amount of from 0.25 to 8.0% by weight.
- the amount of Sb2O3 is from 0 to 2.5% by weight, and the amount of As2O3 is from 0 to 2.5% by weight.
- Antimony and/or arsenic oxides have been found to have a marked effect on the colour of borosilicate glass compositions containing cerium. The antimony and arsenic oxides increase the transmission of the borosilicate glass in the visible part of the spectrum and allow the desired combination of good white light transmission, low ultra-violet light transmission and high radiation stability to be obtained.
- Titanium dioxide in combination with cerium oxide serves to reduce the UV transmission of the glasses and to reduce the tendency of the glasses to darken when exposed to radiation (i.e. it increases the radiation stability of the glass). Incorporation of titanium dioxide in the glass compositions thus makes it possible to use lower cerium levels than would otherwise be necessary. Furthermore, titanium dioxide also reduces melt viscosity more than does cerium oxide, and the presence of titanium dioxide improves melting and refining. However, titanium dioxide also increases visible absorption and this restricts the amount which may be included in the borosilicate glass compositions of the invention.
- the glass compositions comprise up to 2.0% by weight TiO2.
- the amount of TiO2 ranges from 0.25 to 2.0% by weight, and the total amount of TiO2 + CeO2 in the glass composition ranges from 3.5 to 7.0% by weight.
- Alumina helps to improve the chemical durability of the glass composition and helps to inhibit phase separation, but it increases liquidus temperatures, and also darkens the colour of the glasses.
- Zirconia also improves chemical durability, and does not darken the colour as much as alumina, but increases liquidus temperature more than does alumina.
- the glass compositions of the invention comprise up to 3% by weight of Al2O3 + ZrO2.
- the amount of Al2O3 ranges from 0.5 to 3% by weight and the amount of ZrO2 ranges from 0 to 2% by weight.
- B2O3 Boric oxide (B2O3) contents below 10% by weight lead to melting and refining difficulties. Melting and refining of the glass composition improve as boric oxide levels increase, but phase separation can occur if maximum cerium levels coincide with maximum boron levels.
- the total amount of the oxides of lithium, sodium and potassium (defined as R2O above) must be limited to about 6.0% by weight to keep the coefficient of linear thermal expansion of the borosilicate glass close to that of silicon.
- the optimum amount has been found to be approximately 4.5%.
- the minimum amount of R2O is at approximately 3.5% total but melting of the glass components becomes more difficult as alkali levels fall and there is no advantage in seeking to minimise alkali contents.
- the individual alkali metal oxides have different properties. Lithium oxide is the most effective in promoting melting and refining, and also gives good white light transmission, but the tendency to phase separate is aggravated and lithium oxide must not exceed about 1.5% by weight of the glass. Potassium oxide is the least effective in promoting melting and refining and gives darker glasses, but phase separation is minimised. Sodium oxide occupies an intermediate position. A mixture of all three alkali metal oxides offers advantages. If lithium oxide is present above 1% then the maximum sodium oxide level is approximately 3% in order to avoid phase separation.
- Preferred conte nts of the alkali metal oxides are as follows: Li2O 0 to 1.5 % by weight Na2O 0 to 5.5 % by weight K2O 0 to 5.5 % by weight
- zinc oxide and/or alkaline earth metal oxides such as MgO, BaO, CaO and SrO may be added to the batch of glass forming components. These materials are of value in reducing the viscosity of the glass melt when such reduction is required.
- the amount of ZnO added to the batch can be up to 5% by weight; the amount of alkaline earth metal oxides can be up to 5% by weight.
- the borosilicate glass compositions of the invention are prepared using conventional procedures for the preparation of borosilicate glasses. Accordingly specific details of the preparation of the glass compositions are not given herein since a person skilled in the art will readily be able to determine the appropriate processing conditions for preparing the borosilicate glass compositions.
- the low alkali borosilicate glass compositions of the invention provide the desired optical characteristics of good white light transmission, high ultra-violet light absorption and good radiation stability which are required for a glass composition which is to be used as a protective cover for a solar cell.
- a further advantage of the glass compositions of the invention is that the glass compositions are suitable for the manufacture of thin micro-sheet having a thickness of about 50 to 300 microns which is desirable for glass which is to be used as a protective cover for solar cells.
- the present glass compositions also have a coefficient of linear expansion close to that of silicon and possess the added characteristic that they can readily be sealed to a silicon surface.
- the present borosilicate glass compositions readily lend themselves to pretreatments such as cleaning, etching and coating.
- many known borosilicate glass compositions are not suitable for such pretreatments since they have poor chemical durability and a tendency to undergo phase separation if subjected to the said pretreatments.
- Examples in the accompanying Table broadly illustrate the glass compositions of the invention.
- Examples numbers 1, 2, 3, 4, 8, 14, 16, 18 and 26 have been tested for radiation stability by exposing polished samples, thickness between 100 microns and 200 microns, to 5.7 ⁇ 1015 1 MEV electrons in vacuum ( ⁇ 1 ⁇ 10 ⁇ 3 torr) and measuring the loss in visible light transmission. Transmission losses ranged from 1.5% to 4.0% between 400 and 450 nm, which is regarded as satisfactory.
- the thickness of covers for solar cells can range from 50 microns to 300 microns; it is possible for many formulations of glass compositions within the scope of the present invention to be suitable for producing thin glass sheets but unsuitable for producing thick glass sheets, and vice versa .
- the total amount of CeO2 plus TiO2 needs to be high, typically greater than five percent, to give the required UV absorption.
- many of these compositions will be coloured too darkly to be suitable for the thicker covers.
- These high UV absorbing glasses may be bleached to some extent by increasing antimony concentrations to above one percent, but maximum levels of CeO2 + TiO2 (ceria plus titania) are not necessary for the thicker covers (i.e. above about 150 microns in thickness) and it would therefore also be possible to use CeO2 + TiO2 levels below five percent in these cases.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8623214 | 1986-09-26 | ||
GB868623214A GB8623214D0 (en) | 1986-09-26 | 1986-09-26 | Glass compositions |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0261885A1 true EP0261885A1 (de) | 1988-03-30 |
EP0261885B1 EP0261885B1 (de) | 1991-01-23 |
Family
ID=10604853
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87308279A Expired - Lifetime EP0261885B1 (de) | 1986-09-26 | 1987-09-18 | Glaszusammensetzungen |
Country Status (6)
Country | Link |
---|---|
US (1) | US5017521A (de) |
EP (1) | EP0261885B1 (de) |
JP (1) | JPH07100616B2 (de) |
KR (1) | KR950006200B1 (de) |
DE (1) | DE3767633D1 (de) |
GB (1) | GB8623214D0 (de) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0505061A2 (de) * | 1991-03-22 | 1992-09-23 | Pilkington Plc | Borosilicatglaszusammensetzung |
EP0779252A1 (de) | 1995-12-08 | 1997-06-18 | Pilkington Plc | Strahlungsbeständiges Glas und Glasgegenstände |
EP1026130A1 (de) * | 1999-02-05 | 2000-08-09 | Corning Incorporated | Glas für Abdeckung von Sonnenzellen |
EP1059674A2 (de) * | 1999-06-09 | 2000-12-13 | Sharp Kabushiki Kaisha | Abgedeckte Solarzelle und Herstellungsverfahren |
US6262358B1 (en) * | 1999-02-18 | 2001-07-17 | Sharp Kabushiki Kaisha | Solar cell module and solar cell panel using the same |
EP1798775A2 (de) * | 2005-12-17 | 2007-06-20 | Solarwatt Ag | Kristallines photovoltaisches Solarmodul |
EP1805787A2 (de) * | 2004-10-13 | 2007-07-11 | Corning Incorporated | Luftdicht verschlossene glasverpackung und fertigungsverfahren |
DE102009031972A1 (de) | 2009-07-02 | 2011-01-05 | Schott Ag | Photovoltaikmodul |
CN102951841A (zh) * | 2011-08-23 | 2013-03-06 | 扬州通和玻璃有限公司 | 一种太阳能光伏电池用高硼硅玻璃的制备方法 |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4746634A (en) * | 1987-05-28 | 1988-05-24 | Corning Glass Works | Solarization-resistant glass microsheet |
DE4012288C1 (de) * | 1990-04-17 | 1991-07-18 | Schott Glaswerke, 6500 Mainz, De | |
JPH0582822A (ja) * | 1991-09-25 | 1993-04-02 | Nippon Electric Glass Co Ltd | 太陽電池保護カバー |
DE4306004A1 (en) * | 1992-03-19 | 1993-09-23 | Horst Hans Juergen | Silicate glass suitable for working with short wave solid body lasers - contains iron oxide and opt. vanadium and titanium oxide(s) |
DE4230607C1 (de) * | 1992-09-12 | 1994-01-05 | Schott Glaswerke | Chemisch und thermisch hochbelastbares, mit Wolfram verschmelzbares Borosilikatglas und dessen Verwendung |
US5447891A (en) * | 1993-09-29 | 1995-09-05 | Ferro Corporation | Lead-free glaze or enamel for use on ceramic bodies |
FR2728557A1 (fr) | 1994-12-27 | 1996-06-28 | Corning France | Nouveaux verres et lentilles ophtalmiques |
CN1130315C (zh) * | 1995-09-22 | 2003-12-10 | 株式会社村田制作所 | 用于高频电路的具有低介电常数的玻璃组合物 |
JPH0986955A (ja) * | 1995-09-29 | 1997-03-31 | Murata Mfg Co Ltd | 絶縁体用ガラス組成物、絶縁体ペースト、および厚膜印刷回路 |
DE19536708C1 (de) * | 1995-09-30 | 1996-10-31 | Jenaer Glaswerk Gmbh | Zirkon- und lithiumoxidhaltiges Borosilicatglas hoher chemischer Beständigkeit und geringer Viskosität und dessen Verwendung |
US5932502A (en) * | 1996-04-19 | 1999-08-03 | Guardian Industries Corp. | Low transmittance glass |
FR2832811B1 (fr) * | 2001-11-28 | 2004-01-30 | Saint Gobain | Plaque transparente texturee a forte transmission de lumiere |
KR100471651B1 (ko) * | 2002-01-14 | 2005-03-08 | 한국과학기술연구원 | 저온 소성 유전체 세라믹 조성물 및 이의 제조방법 |
DE102004027119A1 (de) * | 2003-06-06 | 2004-12-30 | Schott Ag | UV-Strahlung absorbierendes Glas mit geringer Absorption im sichtbaren Bereich, ein Verfahren zu seiner Herstellung sowie dessen Verwendung |
US7045475B2 (en) * | 2004-04-28 | 2006-05-16 | Pq Corporation | High refractive index glass beads for high retroreflectivity surfaces |
CN101066835B (zh) * | 2007-06-11 | 2010-12-08 | 中国洛阳浮法玻璃集团有限责任公司 | 太阳能超白压延玻璃组分 |
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US9371247B2 (en) | 2009-05-29 | 2016-06-21 | Corsam Technologies Llc | Fusion formable sodium free glass |
CN102503123B (zh) * | 2011-11-24 | 2013-08-21 | 秦皇岛星箭特种玻璃有限公司 | 空间用抗辐照玻璃盖片的制备方法 |
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JP6172445B2 (ja) * | 2013-03-08 | 2017-08-02 | 日本電気硝子株式会社 | カバーガラス |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3499775A (en) * | 1966-07-01 | 1970-03-10 | Owens Illinois Inc | Ultraviolet-absorbing glass compositions containing cerium and molybdenum oxides |
GB1321654A (en) * | 1969-09-29 | 1973-06-27 | Gen Electric | Glass-to-metal seals |
US3843376A (en) * | 1971-04-24 | 1974-10-22 | Philips Corp | Method of manufacturing a mixture for a borosilicate glass |
US4562161A (en) * | 1982-02-20 | 1985-12-31 | Schott Glaswerke | Optical and ophthalmic glass with refractive indices greater than or equal to 1.56, Abbe numbers greater than or equal to 40 and densities less than or equal to 2.70 g/cm3 |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2657146A (en) * | 1951-09-29 | 1953-10-27 | Bausch & Lomb | Borosilicate optical glass |
US3022181A (en) * | 1961-02-01 | 1962-02-20 | Corning Glass Works | Glass color filter |
US3146120A (en) * | 1962-01-11 | 1964-08-25 | American Optical Corp | Absorptive glasses |
US3404015A (en) * | 1965-04-28 | 1968-10-01 | Corning Glass Works | Low thermal expansion glasses |
US3499776A (en) * | 1966-07-13 | 1970-03-10 | Owens Illinois Inc | Alkali metal borosilicate glass compositions containing zirconia |
US3519446A (en) * | 1968-09-19 | 1970-07-07 | Physical Sciences Corp | Ceramic material |
JPS5632347A (en) * | 1979-08-28 | 1981-04-01 | Asahi Glass Co Ltd | Glass for tungsten halogen electric bulb |
FR2550187B1 (fr) * | 1983-08-02 | 1986-06-06 | Corning Glass Works | Verres de faible densite et de haut indice de refraction pour applications ophtalmiques et optiques |
FR2558152B1 (fr) * | 1984-01-13 | 1992-03-27 | Corning Glass Works | Verres a usage ophtalmique de faible densite, absorbant les radiations ultraviolettes et ayant une haute transmission dans le visible et lentilles correctrices constituees de ces verres |
-
1986
- 1986-09-26 GB GB868623214A patent/GB8623214D0/en active Pending
-
1987
- 1987-09-08 US US07/093,601 patent/US5017521A/en not_active Expired - Lifetime
- 1987-09-18 DE DE8787308279T patent/DE3767633D1/de not_active Expired - Lifetime
- 1987-09-18 EP EP87308279A patent/EP0261885B1/de not_active Expired - Lifetime
- 1987-09-24 KR KR1019870010571A patent/KR950006200B1/ko not_active IP Right Cessation
- 1987-09-24 JP JP62239915A patent/JPH07100616B2/ja not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3499775A (en) * | 1966-07-01 | 1970-03-10 | Owens Illinois Inc | Ultraviolet-absorbing glass compositions containing cerium and molybdenum oxides |
GB1321654A (en) * | 1969-09-29 | 1973-06-27 | Gen Electric | Glass-to-metal seals |
US3843376A (en) * | 1971-04-24 | 1974-10-22 | Philips Corp | Method of manufacturing a mixture for a borosilicate glass |
US4562161A (en) * | 1982-02-20 | 1985-12-31 | Schott Glaswerke | Optical and ophthalmic glass with refractive indices greater than or equal to 1.56, Abbe numbers greater than or equal to 40 and densities less than or equal to 2.70 g/cm3 |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0505061A3 (en) * | 1991-03-22 | 1993-05-05 | Pilkington Plc | Borosilicate glass composition |
EP0505061A2 (de) * | 1991-03-22 | 1992-09-23 | Pilkington Plc | Borosilicatglaszusammensetzung |
EP0779252A1 (de) | 1995-12-08 | 1997-06-18 | Pilkington Plc | Strahlungsbeständiges Glas und Glasgegenstände |
US5895719A (en) * | 1995-12-08 | 1999-04-20 | Pilkington Plc | Borosilicate glasses and second surface mirrors thereof |
US6180218B1 (en) | 1995-12-08 | 2001-01-30 | Pilkington Plc | Borosilicate glasses and second surface mirrors thereof |
US6207603B1 (en) | 1999-02-05 | 2001-03-27 | Corning Incorporated | Solar cell cover glass |
EP1026130A1 (de) * | 1999-02-05 | 2000-08-09 | Corning Incorporated | Glas für Abdeckung von Sonnenzellen |
US6262358B1 (en) * | 1999-02-18 | 2001-07-17 | Sharp Kabushiki Kaisha | Solar cell module and solar cell panel using the same |
EP1059674A2 (de) * | 1999-06-09 | 2000-12-13 | Sharp Kabushiki Kaisha | Abgedeckte Solarzelle und Herstellungsverfahren |
US6355875B1 (en) * | 1999-06-09 | 2002-03-12 | Sharp Kabushiki Kaisha | Covered solar cell and manufacturing method thereof |
EP1059674A3 (de) * | 1999-06-09 | 2004-01-21 | Sharp Kabushiki Kaisha | Abgedeckte Solarzelle und Herstellungsverfahren |
US8148179B2 (en) | 2003-04-16 | 2012-04-03 | Corning Incorporated | Hermetically sealed glass package and method of fabrication |
EP1805787A2 (de) * | 2004-10-13 | 2007-07-11 | Corning Incorporated | Luftdicht verschlossene glasverpackung und fertigungsverfahren |
EP1805787A4 (de) * | 2004-10-13 | 2011-02-02 | Corning Inc | Luftdicht verschlossene glasverpackung und fertigungsverfahren |
EP1798775A2 (de) * | 2005-12-17 | 2007-06-20 | Solarwatt Ag | Kristallines photovoltaisches Solarmodul |
EP1798775A3 (de) * | 2005-12-17 | 2008-02-20 | Solarwatt Ag | Kristallines photovoltaisches Solarmodul |
DE102009031972A1 (de) | 2009-07-02 | 2011-01-05 | Schott Ag | Photovoltaikmodul |
DE102009031972B4 (de) * | 2009-07-02 | 2013-01-03 | Schott Ag | Photovoltaikmodul und Verwendung eines Glases für ein Photovoltaikmodul |
CN102951841A (zh) * | 2011-08-23 | 2013-03-06 | 扬州通和玻璃有限公司 | 一种太阳能光伏电池用高硼硅玻璃的制备方法 |
Also Published As
Publication number | Publication date |
---|---|
KR880003841A (ko) | 1988-05-30 |
GB8623214D0 (en) | 1986-10-29 |
KR950006200B1 (ko) | 1995-06-12 |
EP0261885B1 (de) | 1991-01-23 |
JPH07100616B2 (ja) | 1995-11-01 |
JPS6395138A (ja) | 1988-04-26 |
US5017521A (en) | 1991-05-21 |
DE3767633D1 (de) | 1991-02-28 |
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